NO319512B1 - Vandige dispersjoner av polymeriserbare reaktanter og en katalysator, samt fremgangsmate ved fremstilling og anvendelse derav - Google Patents
Vandige dispersjoner av polymeriserbare reaktanter og en katalysator, samt fremgangsmate ved fremstilling og anvendelse derav Download PDFInfo
- Publication number
- NO319512B1 NO319512B1 NO19980672A NO980672A NO319512B1 NO 319512 B1 NO319512 B1 NO 319512B1 NO 19980672 A NO19980672 A NO 19980672A NO 980672 A NO980672 A NO 980672A NO 319512 B1 NO319512 B1 NO 319512B1
- Authority
- NO
- Norway
- Prior art keywords
- catalyst
- water
- mixture
- zinc
- mixture according
- Prior art date
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- 239000003054 catalyst Substances 0.000 title claims description 206
- 239000000376 reactant Substances 0.000 title claims description 34
- 239000006185 dispersion Substances 0.000 title claims description 27
- 238000000034 method Methods 0.000 title claims description 21
- 230000008569 process Effects 0.000 title description 9
- 238000002360 preparation method Methods 0.000 title description 2
- 239000000203 mixture Substances 0.000 claims description 77
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 64
- 238000000576 coating method Methods 0.000 claims description 59
- 239000011248 coating agent Substances 0.000 claims description 40
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 28
- 239000002245 particle Substances 0.000 claims description 28
- 239000000758 substrate Substances 0.000 claims description 16
- 239000007787 solid Substances 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 12
- 229910052751 metal Inorganic materials 0.000 claims description 10
- 239000002184 metal Substances 0.000 claims description 10
- 239000012948 isocyanate Substances 0.000 claims description 8
- 150000002513 isocyanates Chemical class 0.000 claims description 8
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 6
- 229910000323 aluminium silicate Inorganic materials 0.000 claims description 6
- 230000002209 hydrophobic effect Effects 0.000 claims description 6
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 claims description 6
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 5
- 239000010457 zeolite Substances 0.000 claims description 5
- 229910052725 zinc Inorganic materials 0.000 claims description 5
- 239000011701 zinc Substances 0.000 claims description 5
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical group CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 claims description 4
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 claims description 4
- 239000012975 dibutyltin dilaurate Substances 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 239000005909 Kieselgur Substances 0.000 claims description 3
- SPAGIJMPHSUYSE-UHFFFAOYSA-N Magnesium peroxide Chemical compound [Mg+2].[O-][O-] SPAGIJMPHSUYSE-UHFFFAOYSA-N 0.000 claims description 3
- MCMNRKCIXSYSNV-UHFFFAOYSA-N ZrO2 Inorganic materials O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 3
- 229910052797 bismuth Inorganic materials 0.000 claims description 3
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 3
- NSPSPMKCKIPQBH-UHFFFAOYSA-K bismuth;7,7-dimethyloctanoate Chemical compound [Bi+3].CC(C)(C)CCCCCC([O-])=O.CC(C)(C)CCCCCC([O-])=O.CC(C)(C)CCCCCC([O-])=O NSPSPMKCKIPQBH-UHFFFAOYSA-K 0.000 claims description 3
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 150000002540 isothiocyanates Chemical class 0.000 claims description 3
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims description 3
- 239000000454 talc Substances 0.000 claims description 3
- 229910052623 talc Inorganic materials 0.000 claims description 3
- 239000004408 titanium dioxide Substances 0.000 claims description 3
- XMHKTINRBAKEDS-UHFFFAOYSA-N trioctyltin Chemical compound CCCCCCCC[Sn](CCCCCCCC)CCCCCCCC XMHKTINRBAKEDS-UHFFFAOYSA-N 0.000 claims description 3
- 229940012185 zinc palmitate Drugs 0.000 claims description 3
- LPEBYPDZMWMCLZ-CVBJKYQLSA-L zinc;(z)-octadec-9-enoate Chemical compound [Zn+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O LPEBYPDZMWMCLZ-CVBJKYQLSA-L 0.000 claims description 3
- GJAPSKMAVXDBIU-UHFFFAOYSA-L zinc;hexadecanoate Chemical compound [Zn+2].CCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCC([O-])=O GJAPSKMAVXDBIU-UHFFFAOYSA-L 0.000 claims description 3
- ZRWNRAJCPNLYAK-UHFFFAOYSA-N 4-bromobenzamide Chemical compound NC(=O)C1=CC=C(Br)C=C1 ZRWNRAJCPNLYAK-UHFFFAOYSA-N 0.000 claims description 2
- LFDJCUAHUKKNKM-UHFFFAOYSA-K [bis(2-ethylhexanoyloxy)-methylstannyl] 2-ethylhexanoate Chemical compound CCCCC(CC)C(=O)O[Sn](C)(OC(=O)C(CC)CCCC)OC(=O)C(CC)CCCC LFDJCUAHUKKNKM-UHFFFAOYSA-K 0.000 claims description 2
- GVKORIDPEBYOFR-UHFFFAOYSA-K [butyl-bis(2-ethylhexanoyloxy)stannyl] 2-ethylhexanoate Chemical compound CCCCC(CC)C(=O)O[Sn](CCCC)(OC(=O)C(CC)CCCC)OC(=O)C(CC)CCCC GVKORIDPEBYOFR-UHFFFAOYSA-K 0.000 claims description 2
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 claims description 2
- WCEPUHDCWSULDV-UHFFFAOYSA-L bis(trioctylstannyl) benzene-1,2-dicarboxylate Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O.CCCCCCCC[Sn+](CCCCCCCC)CCCCCCCC.CCCCCCCC[Sn+](CCCCCCCC)CCCCCCCC WCEPUHDCWSULDV-UHFFFAOYSA-L 0.000 claims description 2
- RHGQOMYDGHIKFH-GNOQXXQHSA-K bis[[(z)-octadec-9-enoyl]oxy]bismuthanyl (z)-octadec-9-enoate Chemical compound [Bi+3].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O RHGQOMYDGHIKFH-GNOQXXQHSA-K 0.000 claims description 2
- UQOQXWZPXFPRBR-UHFFFAOYSA-K bismuth dodecanoate Chemical compound [Bi+3].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O UQOQXWZPXFPRBR-UHFFFAOYSA-K 0.000 claims description 2
- GRBFCEINWFRDOG-UHFFFAOYSA-K di(octadecanoyloxy)bismuthanyl octadecanoate Chemical compound [Bi+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O GRBFCEINWFRDOG-UHFFFAOYSA-K 0.000 claims description 2
- IRWQVZSQGDKREP-UHFFFAOYSA-L dimethyltin(2+);octadecanoate Chemical compound C[Sn+2]C.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O IRWQVZSQGDKREP-UHFFFAOYSA-L 0.000 claims description 2
- 239000007791 liquid phase Substances 0.000 claims description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 2
- CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical group [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 claims description 2
- 229910052814 silicon oxide Inorganic materials 0.000 claims 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical group [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims 1
- 239000003125 aqueous solvent Substances 0.000 claims 1
- UVKJPLPLHHNSFL-UHFFFAOYSA-N bismuth;ethyl hexanoate Chemical compound [Bi].CCCCCC(=O)OCC UVKJPLPLHHNSFL-UHFFFAOYSA-N 0.000 claims 1
- 239000003575 carbonaceous material Substances 0.000 claims 1
- BFWMWWXRWVJXSE-UHFFFAOYSA-M fentin hydroxide Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(O)C1=CC=CC=C1 BFWMWWXRWVJXSE-UHFFFAOYSA-M 0.000 claims 1
- 239000000243 solution Substances 0.000 claims 1
- 239000011159 matrix material Substances 0.000 description 49
- 239000000839 emulsion Substances 0.000 description 24
- 229920000642 polymer Polymers 0.000 description 23
- 229920005989 resin Polymers 0.000 description 22
- 239000011347 resin Substances 0.000 description 22
- 230000007547 defect Effects 0.000 description 17
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- 230000000694 effects Effects 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 12
- 239000008367 deionised water Substances 0.000 description 10
- 229910021641 deionized water Inorganic materials 0.000 description 10
- -1 objects Substances 0.000 description 10
- 229920001228 polyisocyanate Polymers 0.000 description 10
- 239000005056 polyisocyanate Substances 0.000 description 10
- 230000003111 delayed effect Effects 0.000 description 9
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- 229910000831 Steel Inorganic materials 0.000 description 8
- 239000010959 steel Substances 0.000 description 8
- HJNBKKMVQZKRNU-UHFFFAOYSA-M trioctylstannyl acetate Chemical compound CCCCCCCC[Sn](CCCCCCCC)(CCCCCCCC)OC(C)=O HJNBKKMVQZKRNU-UHFFFAOYSA-M 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 7
- 238000006555 catalytic reaction Methods 0.000 description 7
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- MZZINWWGSYUHGU-UHFFFAOYSA-J ToTo-1 Chemical compound [I-].[I-].[I-].[I-].C12=CC=CC=C2C(C=C2N(C3=CC=CC=C3S2)C)=CC=[N+]1CCC[N+](C)(C)CCC[N+](C)(C)CCC[N+](C1=CC=CC=C11)=CC=C1C=C1N(C)C2=CC=CC=C2S1 MZZINWWGSYUHGU-UHFFFAOYSA-J 0.000 description 6
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- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 4
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- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 3
- 208000032544 Cicatrix Diseases 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 3
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- JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 1
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- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
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- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
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- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
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- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
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- 150000003335 secondary amines Chemical class 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
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- 239000011734 sodium Substances 0.000 description 1
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- 239000012279 sodium borohydride Substances 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
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- 239000007921 spray Substances 0.000 description 1
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- 239000008117 stearic acid Substances 0.000 description 1
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- 239000011975 tartaric acid Substances 0.000 description 1
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- NJRXVEJTAYWCQJ-UHFFFAOYSA-N thiomalic acid Chemical compound OC(=O)CC(S)C(O)=O NJRXVEJTAYWCQJ-UHFFFAOYSA-N 0.000 description 1
- 239000012974 tin catalyst Substances 0.000 description 1
- XATCWUIVPWOLDP-UHFFFAOYSA-N trioctyl(trioctylstannyloxy)stannane Chemical compound CCCCCCCC[Sn](CCCCCCCC)(CCCCCCCC)O[Sn](CCCCCCCC)(CCCCCCCC)CCCCCCCC XATCWUIVPWOLDP-UHFFFAOYSA-N 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
Classifications
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/58—Epoxy resins
- C08G18/581—Reaction products of epoxy resins with less than equivalent amounts of compounds containing active hydrogen added before or during the reaction with the isocyanate component
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/28—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
- B01J20/28002—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their physical properties
- B01J20/28011—Other properties, e.g. density, crush strength
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/30—Processes for preparing, regenerating, or reactivating
- B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/06—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of zinc, cadmium or mercury
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/14—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of germanium, tin or lead
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/16—Catalysts
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/22—Catalysts containing metal compounds
- C08G18/222—Catalysts containing metal compounds metal compounds not provided for in groups C08G18/225 - C08G18/26
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/22—Catalysts containing metal compounds
- C08G18/227—Catalysts containing metal compounds of antimony, bismuth or arsenic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/22—Catalysts containing metal compounds
- C08G18/24—Catalysts containing metal compounds of tin
- C08G18/242—Catalysts containing metal compounds of tin organometallic compounds containing tin-carbon bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/22—Catalysts containing metal compounds
- C08G18/24—Catalysts containing metal compounds of tin
- C08G18/244—Catalysts containing metal compounds of tin tin salts of carboxylic acids
- C08G18/246—Catalysts containing metal compounds of tin tin salts of carboxylic acids containing also tin-carbon bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/12—Adsorbed ingredients, e.g. ingredients on carriers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/44—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications
- C09D5/4488—Cathodic paints
- C09D5/4492—Cathodic paints containing special additives, e.g. grinding agents
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S524/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S524/901—Electrodepositable compositions
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Analytical Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Molecular Biology (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
- Polyurethanes Or Polyureas (AREA)
- Catalysts (AREA)
- Polymerization Catalysts (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Laminated Bodies (AREA)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (2)
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US3862297P | 1997-02-18 | 1997-02-18 | |
US08/995,887 US6669835B1 (en) | 1997-02-18 | 1997-12-22 | Aqueous dispersions of polymerizable reactants and a water incompatible catalyst sorbed on an inorganic particulate carrier |
Publications (3)
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NO980672D0 NO980672D0 (no) | 1998-02-17 |
NO980672L NO980672L (no) | 1998-08-19 |
NO319512B1 true NO319512B1 (no) | 2005-08-22 |
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Family Applications (1)
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NO19980672A NO319512B1 (no) | 1997-02-18 | 1998-02-17 | Vandige dispersjoner av polymeriserbare reaktanter og en katalysator, samt fremgangsmate ved fremstilling og anvendelse derav |
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US (2) | US6669835B1 (de) |
EP (1) | EP0859017B1 (de) |
JP (1) | JP4302790B2 (de) |
KR (1) | KR19980071402A (de) |
CN (1) | CN1304450C (de) |
AR (1) | AR011832A1 (de) |
AT (1) | ATE217639T1 (de) |
AU (1) | AU741570B2 (de) |
BR (1) | BR9800650A (de) |
CA (1) | CA2226661A1 (de) |
DE (1) | DE69805342T2 (de) |
DK (1) | DK0859017T3 (de) |
ES (1) | ES2176909T3 (de) |
HK (1) | HK1015389A1 (de) |
ID (1) | ID20474A (de) |
MX (1) | MXPA98001312A (de) |
MY (1) | MY120315A (de) |
NO (1) | NO319512B1 (de) |
NZ (1) | NZ329779A (de) |
PL (1) | PL324846A1 (de) |
PT (1) | PT859017E (de) |
TR (1) | TR199800238A3 (de) |
TW (1) | TW494118B (de) |
Families Citing this family (20)
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---|---|---|---|---|
US6660781B1 (en) * | 1999-01-05 | 2003-12-09 | Witco Corporation | Process for preparing polyurethane foam |
JP4248898B2 (ja) * | 2003-03-05 | 2009-04-02 | 本田技研工業株式会社 | 鉛フリー電着塗料組成物及び塗装物 |
DE10322466A1 (de) * | 2003-05-16 | 2004-12-02 | Basf Ag | Verfahren zur Herstellung wässriger Polymerisatdispersionen |
EP1654331B1 (de) * | 2003-08-14 | 2013-12-11 | Akzo Nobel Coatings International B.V. | Anstrich enthaltend eine flüssigphase und eine aktivierende pulverphase |
US20060014880A1 (en) * | 2004-07-14 | 2006-01-19 | Qiping Zhong | Nano-talc polymer composites |
KR101505759B1 (ko) * | 2004-08-04 | 2015-03-26 | 포움 서플라이즈 인코포레이션 | 폴리우레탄 폼에서의 반응도 변동 및 촉매 분해 |
US20070045116A1 (en) * | 2005-08-26 | 2007-03-01 | Cheng-Hung Hung | Electrodepositable coating compositions and related methods |
DE102008023444A1 (de) | 2008-05-14 | 2009-11-19 | Basf Coatings Ag | Elektrotauchlackzusammensetzung |
CN102497887A (zh) | 2009-04-17 | 2012-06-13 | Isis创新公司 | 递送遗传物质的组合物 |
DE102010005868A1 (de) | 2010-01-26 | 2011-07-28 | KRONOS INTERNATIONAL, Inc., 51373 | Bismut-haltiges katalytisches System zur Vernetzung von Polymeren |
GB201121070D0 (en) | 2011-12-07 | 2012-01-18 | Isis Innovation | composition for delivery of biotherapeutics |
CN102568854B (zh) * | 2012-03-10 | 2014-05-07 | 辽宁工业大学 | 一种染料敏化太阳能电池的制备方法 |
JP6375304B2 (ja) * | 2012-11-09 | 2018-08-15 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツングBASF Coatings GmbH | リン酸塩汚染された電着塗装塗料組成物で被覆された物品の塗装硬化性の改良方法および電着塗装塗料組成物 |
JP5849943B2 (ja) * | 2012-12-26 | 2016-02-03 | 富士ゼロックス株式会社 | 脂肪酸金属塩粒子の製造方法、脂肪酸金属塩粒子 |
US10221315B2 (en) * | 2013-11-08 | 2019-03-05 | Ppg Industries Ohio, Inc. | Curable film-forming composition comprising catalyst associated with a carrier |
JP6285045B2 (ja) * | 2013-11-19 | 2018-02-28 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツングBASF Coatings GmbH | 酸化マグネシウムを含む導電性基材のための水性ディップコーティング組成物 |
WO2019042696A1 (de) * | 2017-08-30 | 2019-03-07 | Evonik Degussa Gmbh | Verwendung von polyolethern zur herstellung poröser kunststoffbeschichtungen |
JP7248369B2 (ja) * | 2017-11-07 | 2023-03-29 | ピュラック バイオケム ビー. ブイ. | 酢酸塩粉末及びその調製方法 |
EP4363509A1 (de) * | 2021-07-01 | 2024-05-08 | PPG Industries Ohio Inc. | Elektroabscheidbare beschichtungszusammensetzungen |
WO2024082028A1 (en) * | 2022-10-21 | 2024-04-25 | Encap Hive Pty Ltd | Encapsulation and controlled release of liquid polyurethane catalysts |
Family Cites Families (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3114722A (en) | 1958-08-07 | 1963-12-17 | Stauffer Hewitt Inc | Preparation of a composition containing expanded polymeric materials |
DE1127586B (de) | 1958-09-12 | 1962-04-12 | Wacker Chemie Gmbh | Verfahren zum Herstellen von Organopolysiloxanelastomeren aus linearen Organpolysiloxanen |
US3245946A (en) | 1959-04-29 | 1966-04-12 | Union Carbide Corp | Rubber and plastic formulations and process |
NL261966A (de) | 1960-03-03 | 1900-01-01 | ||
DE1203948B (de) | 1961-03-09 | 1965-10-28 | Bayer Ag | Verfahren zur Herstellung von Urethangruppen enthaltenden Schaumstoffen |
NL283771A (de) | 1961-09-29 | |||
US3280489A (en) | 1964-08-06 | 1966-10-25 | Bergmann Conrad | Substitute silver dollar |
US3799854A (en) | 1970-06-19 | 1974-03-26 | Ppg Industries Inc | Method of electrodepositing cationic compositions |
US4017438A (en) | 1974-12-16 | 1977-04-12 | Ppg Industries, Inc. | Ketimine-blocked primary amine group-containing cationic electrodepositable resins |
US4061724A (en) * | 1975-09-22 | 1977-12-06 | Union Carbide Corporation | Crystalline silica |
US4341689A (en) * | 1981-07-02 | 1982-07-27 | Desoto, Inc. | Two component polyurethane coating system having extended pot life and rapid cure |
US4507410A (en) | 1984-02-06 | 1985-03-26 | The Dow Chemical Company | Silica bonded tin urethane catalysts |
US4518718A (en) | 1984-05-18 | 1985-05-21 | The United States Of America As Represented By The United States Department Of Energy | Rigid zeolite containing polyurethane foams |
AU595938B2 (en) | 1986-10-16 | 1990-04-12 | Nippon Paint Co., Ltd. | Electrodeposition coating composition |
US5258071A (en) * | 1987-05-14 | 1993-11-02 | Glaverbel | Vitreous filler material for a polymeric matrix |
GB8729069D0 (en) * | 1987-12-12 | 1988-01-27 | Rapra Techn Ltd | Temperature activated catalysts for liquid polymer cures |
US5178748A (en) * | 1988-12-22 | 1993-01-12 | Imperial Chemical Industries | Catalytic reactions using zeolites |
US5177117A (en) | 1989-05-01 | 1993-01-05 | Air Products And Chemicals, Inc. | Controlled release catalysts and curing agents for making polyurethane and/or polyisocyanurate product |
US5168084A (en) * | 1990-05-07 | 1992-12-01 | Uop | Molecular sieve agglomerates with improved transport properties |
US5116914A (en) | 1990-12-18 | 1992-05-26 | E. I. Du Pont De Nemours And Company | Cathodic electrodeposition coatings containing alkyl metal acetonate catalyst |
US5218211A (en) | 1991-10-23 | 1993-06-08 | The United States Of America As Represented By The Secretary Of Commerce | System for sampling the sizes, geometrical distribution, and frequency of small particles accumulating on a solid surface |
US5356529A (en) | 1993-05-03 | 1994-10-18 | Ppg Industries, Inc. | Electrodepositable compositions containing triorganotin catalysts |
US5718817A (en) * | 1993-07-28 | 1998-02-17 | Elf Atochem North America, Inc. | Catalyst for low temperature cure of blocked isocyanates |
US5488092A (en) * | 1994-04-26 | 1996-01-30 | Gencorp Inc. | Low VOC, primerless, polyurethane compostions |
US5672432A (en) * | 1995-11-16 | 1997-09-30 | Basf Corportion | Cathodic electrocoat compositions containing self-crosslinking polymers |
-
1997
- 1997-12-22 US US08/995,887 patent/US6669835B1/en not_active Expired - Lifetime
-
1998
- 1998-02-13 CA CA002226661A patent/CA2226661A1/en not_active Abandoned
- 1998-02-16 AU AU53943/98A patent/AU741570B2/en not_active Expired
- 1998-02-17 PL PL98324846A patent/PL324846A1/xx unknown
- 1998-02-17 TR TR1998/00238A patent/TR199800238A3/tr unknown
- 1998-02-17 KR KR1019980004690A patent/KR19980071402A/ko not_active Application Discontinuation
- 1998-02-17 TW TW087102200A patent/TW494118B/zh not_active IP Right Cessation
- 1998-02-17 NO NO19980672A patent/NO319512B1/no unknown
- 1998-02-17 NZ NZ329779A patent/NZ329779A/xx not_active IP Right Cessation
- 1998-02-17 MX MXPA98001312A patent/MXPA98001312A/es active IP Right Grant
- 1998-02-17 MY MYPI98000654A patent/MY120315A/en unknown
- 1998-02-18 ES ES98301178T patent/ES2176909T3/es not_active Expired - Lifetime
- 1998-02-18 PT PT98301178T patent/PT859017E/pt unknown
- 1998-02-18 DE DE69805342T patent/DE69805342T2/de not_active Expired - Lifetime
- 1998-02-18 CN CNB98105210XA patent/CN1304450C/zh not_active Expired - Lifetime
- 1998-02-18 AT AT98301178T patent/ATE217639T1/de not_active IP Right Cessation
- 1998-02-18 BR BR9800650-9A patent/BR9800650A/pt not_active IP Right Cessation
- 1998-02-18 AR ARP980100727A patent/AR011832A1/es unknown
- 1998-02-18 JP JP05126198A patent/JP4302790B2/ja not_active Expired - Lifetime
- 1998-02-18 EP EP98301178A patent/EP0859017B1/de not_active Expired - Lifetime
- 1998-02-18 DK DK98301178T patent/DK0859017T3/da active
- 1998-02-18 ID IDP980218A patent/ID20474A/id unknown
-
1999
- 1999-01-27 HK HK99100354A patent/HK1015389A1/xx not_active IP Right Cessation
-
2003
- 2003-07-30 US US10/630,034 patent/US7138044B2/en not_active Expired - Fee Related
Also Published As
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NZ329779A (en) | 1999-07-29 |
TR199800238A2 (xx) | 1998-09-21 |
KR19980071402A (ko) | 1998-10-26 |
BR9800650A (pt) | 1999-12-14 |
US7138044B2 (en) | 2006-11-21 |
ATE217639T1 (de) | 2002-06-15 |
MY120315A (en) | 2005-10-31 |
US6669835B1 (en) | 2003-12-30 |
PT859017E (pt) | 2002-10-31 |
DE69805342T2 (de) | 2002-11-14 |
JP4302790B2 (ja) | 2009-07-29 |
ES2176909T3 (es) | 2002-12-01 |
NO980672L (no) | 1998-08-19 |
US20040024116A1 (en) | 2004-02-05 |
TW494118B (en) | 2002-07-11 |
HK1015389A1 (en) | 1999-10-15 |
NO980672D0 (no) | 1998-02-17 |
MXPA98001312A (es) | 2005-07-15 |
AR011832A1 (es) | 2000-09-13 |
JPH10330410A (ja) | 1998-12-15 |
TR199800238A3 (tr) | 1998-09-21 |
CN1197081A (zh) | 1998-10-28 |
CA2226661A1 (en) | 1998-08-18 |
DK0859017T3 (da) | 2002-09-09 |
EP0859017B1 (de) | 2002-05-15 |
AU5394398A (en) | 1998-08-20 |
DE69805342D1 (de) | 2002-06-20 |
CN1304450C (zh) | 2007-03-14 |
PL324846A1 (en) | 1998-08-31 |
AU741570B2 (en) | 2001-12-06 |
EP0859017A1 (de) | 1998-08-19 |
ID20474A (id) | 1998-12-24 |
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